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水合磷酸氧钒正极水系锌电池的储能性能

邵琪瑶 丁玟淇 孙震 蔡翔

大连工业大学学报2026,Vol.45Issue(2):109-116,8.
大连工业大学学报2026,Vol.45Issue(2):109-116,8.DOI:10.19670/j.cnki.dlgydxxb.2026.0205

水合磷酸氧钒正极水系锌电池的储能性能

Energy storage performance of aqueous zinc-ion batteries with hydrated vanadyl phosphate cathode

邵琪瑶 1丁玟淇 1孙震 2蔡翔1

作者信息

  • 1. 大连工业大学 轻工与化学工程学院,辽宁 大连 116034
  • 2. 鞍山师范学院化学与生命科学学院,辽宁鞍山 114005
  • 折叠

摘要

Abstract

To explore the mechanism and overcoming methods for rapid function failure of polyanionic compounds in the application of aqueous zinc batteries,which were with high electrode potentials.The electrochemical performance of hydrated vanadyl phosphate,as a type of model cathode material,was systematically investigated in ZnSO4 and ZnCl2 electrolytes with varying concentrations,as well as in a mixed ZnCl2-H3 PO4 electrolyte.The results indicated that the function failure of hydrated vanadyl phosphate was primarily attributing to dissolution of vanadium and loss of PO 43-,which induced an irreversible phase transformation reaction.The dissolution of vanadium shortened the electrode lifespan,while the loss of PO43-led to the disappearance of the high-potential charge/discharge plateau.ZnCl2 with high concentration would reduce the activity of free water,thereby suppressed the dissolution of vanadium,while the introduction of H3PO4 lowered the thermodynamic spontaneity of the reaction.In the mixed electrolyte consisting of 10 mol/kg ZnCl2 and 0.5 mol/kg H3PO4,the specific capacity of hydrated vanadyl phosphate electrode was up to 61 mA·h/g,whose capacity retention reached 130%after 50 galvanostatic charge-discharge cycles.All of the results confirmed the enhanced cycling stability.

关键词

水系锌电池/水合磷酸氧钒/盐包水电解液/降解机制

Key words

aqueous zinc batteries/hydrated vanadyl phosphate/water-in-salt electrolytes/degrada-tion mechanisms

分类

化学化工

引用本文复制引用

邵琪瑶,丁玟淇,孙震,蔡翔..水合磷酸氧钒正极水系锌电池的储能性能[J].大连工业大学学报,2026,45(2):109-116,8.

基金项目

辽宁省自然科学基金项目(2023-BS-173) (2023-BS-173)

辽宁省教育厅基本科研项目(LJKQZ20222291). (LJKQZ20222291)

大连工业大学学报

1674-1404

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